Evidence map›Paper›PMID 42204451›Full record

ArticleBMC plant biology2026

Species-specific, accession-specific, and common responses of foliar phytohormones and morphological traits to drought and herbivory.

Xue Xiao, Kruthika Sen Aragam, Andrea Bräutigam, Thomas Dussarrat, Selina Gaar, Maximilian Hanusch, Robin Heinen, Marvin Hildebrandt, Ruth Jakobs, Robert R Junker and 14 more

Abstract read
In one paragraph

Article in BMC plant biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Xue XiaoDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany. xue.xiao@uni-bielefeld.de.
Kruthika Sen AragamDepartment of Molecular Botany, Institute of Biology, University of Hohenheim, Stuttgart, 70599, Germany.
Andrea BräutigamDepartment of Computational Biology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, 33615, Germany.
Thomas DussarratDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany.
Selina GaarDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany.
Maximilian HanuschDepartment of Biology, Evolutionary Ecology of Plants, Marburg University, Marburg, 35043, Germany.
Robin HeinenDepartment for Life Science Systems, School of Life Sciences, Terrestrial Ecology Research Group, Technical University of Munich, Freising, 85354, Germany.
Marvin HildebrandtDepartment of Computational Biology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, 33615, Germany.
Ruth JakobsDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany.
Robert R JunkerDepartment of Biology, Evolutionary Ecology of Plants, Marburg University, Marburg, 35043, Germany.
Radhika KeshanDepartment of Molecular Botany, Institute of Biology, University of Hohenheim, Stuttgart, 70599, Germany.
Judit V Mendoza ServínLeibniz Institute of Vegetable and Ornamental Crops (IGZ), Großbeeren, 14797, Germany.
Elikplim A SetordjieDepartment for Life Science Systems, School of Life Sciences, Terrestrial Ecology Research Group, Technical University of Munich, Freising, 85354, Germany.
Yonca B SeymenResearch Unit Environmental Simulation, Helmholtz Munich, Neuherberg, 85764, Germany.
Anke SteppuhnDepartment of Molecular Botany, Institute of Biology, University of Hohenheim, Stuttgart, 70599, Germany.
Sybille B UnsickerDepartment of Plant-Environment-Interactions, Kiel University, Kiel, 24118, Germany.
Nicole M van DamLeibniz Institute of Vegetable and Ornamental Crops (IGZ), Großbeeren, 14797, Germany.
Baris WeberResearch Unit Environmental Simulation, Helmholtz Munich, Neuherberg, 85764, Germany.
Sarah K WeirauchDepartment of Plant-Environment-Interactions, Kiel University, Kiel, 24118, Germany.
Wolfgang W WeisserDepartment for Life Science Systems, School of Life Sciences, Terrestrial Ecology Research Group, Technical University of Munich, Freising, 85354, Germany.
Dominik ZiajaDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany.
Jörg-Peter SchnitzlerResearch Unit Environmental Simulation, Helmholtz Munich, Neuherberg, 85764, Germany.
J Barbro WinklerResearch Unit Environmental Simulation, Helmholtz Munich, Neuherberg, 85764, Germany.
Caroline MüllerDepartment of Chemical Ecology, Bielefeld University, Bielefeld, 33615, Germany. caroline.mueller@uni-bielefeld.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlants are exposed to various environmental challenges. Especially with ongoing climate change, droughts and insect outbreaks are expected to become more frequent. Plant responses to these challenges are mediated by interacting phytohormonal pathways that influence plant growth, but little is known how these responses to single and combined challenges vary across different scales, within and between species. Thus, we investigated species- and accession-specific responses to two environmental challenges in three perennial plant species and compared the responses between species. Clones of several accessions of the herbaceous species Tanacetum vulgare, the woody vine Solanum dulcamara, and the tree Populus nigra were subjected to similar control, herbivory, drought, and combined (drought and herbivory) treatments. After the exposure, foliar phytohormones and various morphological traits were quantified.

resultsPlants of T. vulgare did not respond in jasmonic acid (JA) levels, but showed an increase in abscisic acid (ABA) and a reduced aboveground biomass, particularly under the combined challenges. Plants of S. dulcamara exhibited similar responses, but JA levels were enhanced by all treatments. In contrast, P. nigra uniquely induced salicylic acid under the combined treatment, but showed no impacts on growth. Phenotypic plasticity reflected these species-specific patterns, with none of the phytohormones or morphological traits exhibiting uniform plasticity across species, but with substantial accession-specific pattern. Structural equation models further revealed distinct phytohormone-mediated pathways underlying morphological traits, potentially linking environmental challenges and accessions to specific plant responses within each species. Besides these species-specific differences, several traits responded consistently in all three species to the environmental challenges. Jasmonoyl-isoleucine was induced by herbivory and the combined treatment, ABA by drought and the combined treatment, and indole acetic acid by the combined treatment in all species. Root mass remained unchanged in all species.

conclusionsOur results indicate that plant responses to similar challenges include both species-specific and conserved components. The combined treatment elicited the strongest responses, suggesting that simultaneous challenges under climate change may have complex effects on plant performance. The intra- and interspecific differences revealed here highlight the need to further explore the mechanisms underlying this specificity and understand patterns of plant resilience.

Indexed as

DroughtsHerbivoryPlant Growth RegulatorsPopulusSolanumAbscisic AcidAnimalsCyclopentanesDrought ResistanceOxylipinsPlant LeavesSpecies SpecificityAbscisic AcidCyclopentanesjasmonic acidOxylipinsPlant Growth RegulatorsClimate changeEnvironmental stressorsHormonal signalingInduced plant responsesPerennialsPhenotypic plasticity

Identifiers

PMID42204451
PMCPMC13217867

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.